# FDA recall Z-0972-2018

> **Medimop Medical Projects Ltd.** · Class II · device recall initiated 2017-10-06.

## Product

Vial2BagDC, Product Number 6070112.   The 20mm Vial2Bag DC device, is intended for use in  healthcare facilities or in-home environment by the patient  or care-giver to aid and support prescribed treatment and  therapy. The device consists of the Vial2Bag piercing  spike and cover, the IV Port connector and an integrated  Vial Adapter (20mm) for access to the drug/solution vial.

## Reason for recall

Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag  DC body during the drug reconstitution I IV Set attachment process.

## Distribution

US Distribution

## Key facts

- **Recall number:** Z-0972-2018
- **Recalling firm:** Medimop Medical Projects Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-06
- **Report date:** 2018-03-21
- **Termination date:** 2024-01-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Raanana, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0972-2018

## Citation

> AI Analytics. FDA recall Z-0972-2018. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-0972-2018. Source: US FDA. Licensed CC0.

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